DR info

Clinical trials : 447 / Drugs : 297 - (DrugBank : 57) / Drug target genes : 52 - Drug target pathways : 146

Juvenile idiopathic arthritis and other diseases between which drug repositioning might occur (Sakate and Kimura 2021) . Circle size: Number of drugs, Line breadth: Drug repositionability

ID	Diseases (Sorted by drug repositionability)
107	Juvenile idiopathic arthritis
46	Malignant rheumatoid arthritis
13	Multiple sclerosis/Neuromyelitis optica
97	Ulcerative colitis
96	Crohn disease
50	Dermatomyositis
271	Ankylosing spondylitis
51	Scleroderma
6	Parkinson disease
65	Primary immunodeficiency
53	Sjogren syndrome
2	Amyotrophic lateral sclerosis
84	Sarcoidosis
49	Systemic lupus erythematosus
113	Muscular dystrophy
41	Giant cell arteritis
56	Behcet disease
11	Myasthenia gravis
226	Interstitial cystitis with Hunners ulcer
162	Pemphigoid
38	Stevens-Johnson syndrome
40	Takayasu arteritis
55	Relapsing polychondritis
299	Cystic fibrosis
222	Primary nephrotic syndrome
60	Aplastic anemia
269	Pyogenic arthritis
58	Hypertrophic cardiomyopathy
28	Systemic amyloidosis
19	Lysosomal storage disease
228	Bronchiolitis obliterans
93	Primary biliary cholangitis
284	Diamond-Blackfan anemia
256	Muscle glycogenosis
224	Purpura nephritis
164	Oculocutaneous albinism
34	Neurofibromatosis
285	Fanconi anemia
286	Hereditary sideroblastic anemia
95	Autoimmune hepatitis
39	Toxic epidermal necrolysis
270	Chronic recurrent multifocal osteomyelitis
151	Rasmussen encephalitis
231	Alpha-1-antitrypsin deficiency
66	IgA nephropathy
86	Pulmonary arterial hypertension
44	Wegener granulomatosis
298	Hereditary pancreatitis
8	Huntington disease
45	Eosinophilic granulomatosis with Polyangiitis
160	Congenital ichthyosis
283	Acquired pure red cell aplasia
63	Idiopathic thrombocytopenic purpura
36	Epidermolysis bullosa
42	Polyarteritis nodosa
302	Leber hereditary optic neuropathy
300	IgG4-related disease
326	Osteopetrosis
85	Idiopathic interstitial pneumonia
78	Hypopituitarism
70	Spinal stenosis
21	Mitochondrial disease
168	Ehlers-Danlos syndrome
106	Cryopyrin-associated periodic syndrome
274	Osteogenesis Imperfecta
62	Paroxysmal nocturnal hemoglobinuria
35	Pemphigus
323	Aromatic L-amino acid decarboxylase deficiency
90	Retinitis pigmentosa
20	Adrenoleukodystrophy
158	Tuberous sclerosis
1	Spinal and bulbar muscular atrophy
64	Thrombotic thrombocytopenic purpura
26	HTLV-1-associated myelopathy
61	Autoimmune hemolytic anemia
265	Lipodystrophy
10	Charcot-Marie-Tooth disease
234	Peroxisomal disease (except Adrenoleukodystrophy)
251	Urea cycle disorder
43	Microscopic polyangiitis
266	Familial mediterranean fever
280	Huge arteriovenous malformation with cervicofacial or limb lesion
227	Osler disease
268	Nakajo-Nishimura syndrome
325	Hereditary autoinflammatory syndrome
337	Homocystinuria
257	Hepatic glycogenosis
282	Congenital dyserythropoietic anemia
193	Prader-Willi syndrome
114	Non-dystrophic myotonia syndrome
288	Autoimmune acquired coagulation factor deficiency
15	Inclusion body myositis
236	Pseudohypoparathyroidism
37	Generalised pustular psoriasis
127	Frontotemporal lobar degeneration
98	Eosinophilic gastrointestinal disease
172	Hypophosphatasia
22	Moyamoya disease
118	Myelomeningocele
212	Tricuspid atresia
331	Idiopathic multicentric castleman disease
5	Progressive supranuclear palsy
246	Methylmalonic acidemia
169	Menkes disease
170	Occipital horn syndrome
254	Porphyria
238	Vitamin D-resistant rickets
235	Hypoparathyroidism
71	Idiopathic osteonecrosis of the femoral head
108	TNF receptor-associated periodic syndrome
267	Hyper-IgD syndrome
317	Trifunctional protein deficiency
54	Adult still disease
191	Werner syndrome
220	Rapidly progressive glomerulonephritis
30	Distal myopathy